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| http://dx.doi.org/10.1159/000534080 | DOI Listing |
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European Autism GEnomics Registry (EAGER): protocol for a multicentre cohort study and registry.
BMJ Open
June 2024
Department of Psychology, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
Article Synopsis
- Autism is a common condition influenced by both single gene issues and multiple genes, and many autistic people need better healthcare that genomics can help provide.
- The European Autism GEnomics Registry (EAGER) aims to collect info about autistic people who have had their entire DNA sequenced to help with future research and trials.
- EAGER will involve 1,500 participants from 13 places in 8 countries who will share genetic samples and fill out surveys to help researchers understand the link between genetics and health.
Just Dissemination of Genomics-Informed Public Health Applications: Time to Deepen Our Public Engagement Approaches.
Public Health Genomics
December 2023
Department of Behavioral, Social, and Health Education Sciences, Rollins School of Public Health, Emory University, Atlanta, Georgia, USA.
Blending Insights from Implementation Science and the Social Sciences to Mitigate Inequities in Screening for Hereditary Cancer Syndromes.
Int J Environ Res Public Health
October 2019
Division of Cancer Control and Population Sciences, National Cancer Institute, 9609 Medical Center Drive, Rockville, MD 20850, USA.
Genomic screening to identify people at high risk for adult-onset hereditary conditions has potential to improve population health. However, if not equitably accessible, genomics-informed screening programs will exacerbate existing health inequities or give rise to new ones. To realize the disease prevention potential of these screening tools, we need strategies to broaden their reach.
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